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Arquivos De Neuro-Psiquiatria|August 17, 2022
Gene therapy in neuromuscular disordersRodrigo Holanda Mendonça, Edmar ZanoteliArquivos De Neuro-Psiquiatria|December 20, 2024
A self-reported Brazilian registry of 5q-spinal muscular atrophy: data on natural history, genetic characteristics, and multidisciplinary careRodrigo Holanda Mendonça, Juliane Suellen Arndt de Godoi, Edmar ZanoteliUltrasound in Medicine & Biology|April 10, 2023
Muscle Ultrasound Changes Correlate With Functional Impairment in Spinal Muscular AtrophyAna Lucila Moreira, Rodrigo Holanda Mendonça, Graziela Jorge Polido, et al.Neuromuscular Disorders : NMD|April 7, 2021
Motor unit number index (MUNIX) in children and adults with 5q-spinal muscular atrophy: Variability and clinical correlationsRodrigo Holanda Mendonça, Ligia Maria Sotero Machado, Carlos Otto Heise, et al.Gene Therapy|June 5, 2024
Gene replacement therapy for spinal muscular atrophy: safety and preliminary efficacy in a Brazilian cohortRodrigo Holanda Mendonça, Adriana Banzzatto Ortega, Ciro Matsui, et al.Lancet Regional Health. Americas|August 8, 2025
Safety and tolerability of onasemnogene abeparvovec for patients with spinal muscular atrophy weighing ≤17 kg and ≤24 months old from OFELIA, a phase 4, open-label, multicenter, non-randomised, interventional studyJonas Alex Saute, Javier Muntadas, Juliana Gurgel-Giannetti, et al.Arquivos De Neuro-Psiquiatria|March 19, 2025
Brazilian Portuguese version of the revised upper-limb module: cross-cultural adaptation and validationMariana Cunha Artilheiro, Juliana Rodrigues Iannicelli, Graziela Jorge Polido, et al.Arquivos De Neuro-Psiquiatria|May 10, 2018
Therapeutic advances in 5q-linked spinal muscular atrophyUmbertina Conti Reed, Edmar ZanoteliNeurology|January 2, 2024
Unraveling the Genetic Tapestry of a Village LegendMarcos Vinícius Oliveira Marques, Edmar ZanoteliArquivos De Neuro-Psiquiatria|February 7, 2024
Gene-based therapies for neuromuscular disordersEdmar Zanoteli, Marcondes Cavalcante França, Wilson MarquesPageof 16